US20190231360A1 - Packing Coil - Google Patents
Packing Coil Download PDFInfo
- Publication number
- US20190231360A1 US20190231360A1 US16/380,917 US201916380917A US2019231360A1 US 20190231360 A1 US20190231360 A1 US 20190231360A1 US 201916380917 A US201916380917 A US 201916380917A US 2019231360 A1 US2019231360 A1 US 2019231360A1
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- US
- United States
- Prior art keywords
- loop portions
- open loop
- closed loop
- microcoil
- occlusion device
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
- 238000012856 packing Methods 0.000 title description 9
- 238000004804 winding Methods 0.000 claims description 21
- 206010002329 Aneurysm Diseases 0.000 description 19
- BASFCYQUMIYNBI-UHFFFAOYSA-N platinum Chemical compound [Pt] BASFCYQUMIYNBI-UHFFFAOYSA-N 0.000 description 12
- 238000011282 treatment Methods 0.000 description 8
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- 230000010102 embolization Effects 0.000 description 5
- 229910052697 platinum Inorganic materials 0.000 description 5
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- 229910001069 Ti alloy Inorganic materials 0.000 description 2
- RTAQQCXQSZGOHL-UHFFFAOYSA-N Titanium Chemical compound [Ti] RTAQQCXQSZGOHL-UHFFFAOYSA-N 0.000 description 2
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- 229910000679 solder Inorganic materials 0.000 description 2
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- 201000008450 Intracranial aneurysm Diseases 0.000 description 1
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- 208000007536 Thrombosis Diseases 0.000 description 1
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- BABWHSBPEIVBBZ-UHFFFAOYSA-N diazete Chemical compound C1=CN=N1 BABWHSBPEIVBBZ-UHFFFAOYSA-N 0.000 description 1
- 238000006073 displacement reaction Methods 0.000 description 1
- 229940012952 fibrinogen Drugs 0.000 description 1
- 238000013467 fragmentation Methods 0.000 description 1
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- PCHJSUWPFVWCPO-UHFFFAOYSA-N gold Chemical compound [Au] PCHJSUWPFVWCPO-UHFFFAOYSA-N 0.000 description 1
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- WUAPFZMCVAUBPE-UHFFFAOYSA-N rhenium atom Chemical compound [Re] WUAPFZMCVAUBPE-UHFFFAOYSA-N 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- 239000010948 rhodium Substances 0.000 description 1
- MHOVAHRLVXNVSD-UHFFFAOYSA-N rhodium atom Chemical compound [Rh] MHOVAHRLVXNVSD-UHFFFAOYSA-N 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000010935 stainless steel Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
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- 229910052715 tantalum Inorganic materials 0.000 description 1
- GUVRBAGPIYLISA-UHFFFAOYSA-N tantalum atom Chemical compound [Ta] GUVRBAGPIYLISA-UHFFFAOYSA-N 0.000 description 1
- 230000001225 therapeutic effect Effects 0.000 description 1
- 230000002885 thrombogenetic effect Effects 0.000 description 1
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Images
Classifications
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61M—DEVICES FOR INTRODUCING MEDIA INTO, OR ONTO, THE BODY; DEVICES FOR TRANSDUCING BODY MEDIA OR FOR TAKING MEDIA FROM THE BODY; DEVICES FOR PRODUCING OR ENDING SLEEP OR STUPOR
- A61M29/00—Dilators with or without means for introducing media, e.g. remedies
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
- A61B17/1214—Coils or wires
- A61B17/12145—Coils or wires having a pre-set deployed three-dimensional shape
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- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
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- A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
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- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12109—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel
- A61B17/12113—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder in a blood vessel within an aneurysm
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12099—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder
- A61B17/12122—Occluding by internal devices, e.g. balloons or releasable wires characterised by the location of the occluder within the heart
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- A61B17/12—Surgical instruments, devices or methods, e.g. tourniquets for ligaturing or otherwise compressing tubular parts of the body, e.g. blood vessels, umbilical cord
- A61B17/12022—Occluding by internal devices, e.g. balloons or releasable wires
- A61B17/12131—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device
- A61B17/12168—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device having a mesh structure
- A61B17/12172—Occluding by internal devices, e.g. balloons or releasable wires characterised by the type of occluding device having a mesh structure having a pre-set deployed three-dimensional shape
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61F—FILTERS IMPLANTABLE INTO BLOOD VESSELS; PROSTHESES; DEVICES PROVIDING PATENCY TO, OR PREVENTING COLLAPSING OF, TUBULAR STRUCTURES OF THE BODY, e.g. STENTS; ORTHOPAEDIC, NURSING OR CONTRACEPTIVE DEVICES; FOMENTATION; TREATMENT OR PROTECTION OF EYES OR EARS; BANDAGES, DRESSINGS OR ABSORBENT PADS; FIRST-AID KITS
- A61F2/00—Filters implantable into blood vessels; Prostheses, i.e. artificial substitutes or replacements for parts of the body; Appliances for connecting them with the body; Devices providing patency to, or preventing collapsing of, tubular structures of the body, e.g. stents
- A61F2/01—Filters implantable into blood vessels
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- A—HUMAN NECESSITIES
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- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/0057—Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect
- A61B2017/00575—Implements for plugging an opening in the wall of a hollow or tubular organ, e.g. for sealing a vessel puncture or closing a cardiac septal defect for closure at remote site, e.g. closing atrial septum defects
- A61B2017/00592—Elastic or resilient implements
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B2017/00831—Material properties
- A61B2017/00867—Material properties shape memory effect
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- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/42—Gynaecological or obstetrical instruments or methods
- A61B2017/4233—Operations on Fallopian tubes, e.g. sterilization
Definitions
- the present invention relates to devices for the occlusion of body cavities, such as the embolization of vascular aneurysms and the like, and methods for making and using such devices.
- the occlusion of body cavities, blood vessels, and other lumina by embolization is desired in a number of clinical situations.
- the occlusion of fallopian tubes for the purposes of sterilization, and the occlusive repair of cardiac defects, such as a patent foramen ovale, patent ductus arteriosis, and left atrial appendage, and atrial septal defects are desired in a number of clinical situations.
- the occlusion of fallopian tubes for the purposes of sterilization and the occlusive repair of cardiac defects, such as a patent foramen ovale, patent ductus arteriosis, and left atrial appendage, and atrial septal defects.
- the function of an occlusion device in such situations is to substantially block or inhibit the flow of bodily fluids into or through the cavity, lumen, vessel, space, or defect for the therapeutic benefit of the patient.
- vascular embolization has been used to control vascular bleeding, to occlude the blood supply to tumors, and to occlude vascular aneurysms, particularly intracranial aneurysms.
- vascular embolization for the treatment of aneurysms has received much attention.
- thrombogenic microcoils may be made of biocompatible metal alloy(s) (typically a radio-opaque material such as platinum or tungsten) or a suitable polymer. Examples of microcoils are disclosed in the following patents: U.S. Pat.
- GDC Guglielmi Detachable Coil
- the GDC employs a platinum wire coil fixed to a stainless steel delivery wire by a solder connection. After the coil is placed inside an aneurysm, an electrical current is applied to the delivery wire, which electrolytically disintegrates the solder junction, thereby detaching the coil from the delivery wire. The application of current also creates a positive electrical charge on the coil, which attracts negatively-charged blood cells, platelets, and fibrinogen, thereby increasing the thrombogenicity of the coil.
- Several coils of different diameters and lengths can be packed into an aneurysm until the aneurysm is completely filled. The coils thus create and hold a thrombus within the aneurysm, inhibiting its displacement and its fragmentation.
- the present invention provides a more advanced and improved occlusion device, for example an occlusion device in the form of a neuro-embolic microcoil, that exhibits greater stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for treating and occluding the target site.
- the occlusion device comprises a microcoil having a relaxed configuration comprising a plurality of open loop portions interposed between a plurality of closed loop portions.
- the occlusion device comprises a microcoil having a relaxed configuration comprising a plurality of open loop portions interposed between a plurality of closed loop portions, each of the plurality of open looped portions formed substantially within a different plane.
- the present invention provides a method for occluding a body cavity comprising passing a delivery system through a vasculature until a distal end of the delivery system is positioned at a target location; advancing a first portion of the occlusion device from the distal end of the delivery system into the target site, the first portion forming a closed loop when the occlusion device is in a relaxed state; advancing a second portion of the occlusion device from the distal end of the delivery system into the target site, the second portion forming at least one open loop when the occlusion device is in a relaxed state; advancing a third portion of the occlusion device from the distal end of the delivery system into the target site, the first portion forming a closed loop when the occlusion device is in a relaxed state; and releasing the occlusion device from the delivery system and withdrawing the delivery system from the vasculature.
- FIG. 1 is a perspective view of a portion of a microcoil employed to form a device according to the present invention
- FIG. 2 is a perspective view of device according to one embodiment of the present invention.
- FIG. 3 is a perspective view of a device on a mandrel employed to fabricate the device according to one embodiment of the present invention
- FIG. 4 is a perspective view of a device according to one embodiment of the present invention.
- FIGS. 5A through 5C are perspective views of a device on a mandrel employed to fabricate the device according to one embodiment of the present invention.
- FIG. 6 is a perspective view of a device according to one embodiment of the present invention.
- FIG. 7A is a perspective view of a device according to one embodiment of the present invention.
- FIG. 7B is a perspective view of a mandrel employed to fabricate a device according to one embodiment of the present invention.
- FIG. 7C is a perspective view of a device on a mandrel according to one embodiment of the present invention.
- FIG. 8A is a perspective view of a device according to one embodiment of the present invention.
- FIG. 8B is a perspective view of a mandrel employed to fabricate a device according to one embodiment of the present invention.
- FIG. 8C is a perspective view of a device on a mandrel according to one embodiment of the present invention.
- FIG. 9 is a perspective view of a device according to one embodiment of the present invention.
- FIG. 10 is a perspective view of a device according to one embodiment of the present invention.
- FIG. 11 is a table describing various configurations of a device according to one embodiment of the present invention.
- FIG. 12 is a perspective view of a device according to one embodiment of the present invention.
- Devices or packing coils according to the present invention provide improved stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for occlusion and treatment of the target site.
- these objectives are achieved by employing a microcoil having a relaxed, low-energy state configuration incorporating both closed loop portions and open loop portions.
- devices or packing coils according to the present invention are formed of a suitable length of wire 12 formed into a primary winding in the shape of a helical microcoil 14 .
- Suitable materials for the wire 12 include platinum, rhodium, palladium, rhenium, tungsten, gold, silver, tantalum, and various alloys of these metals.
- Various surgical grade stainless steels may also be used.
- Preferred materials include the platinum/tungsten alloy known as Platinum 479 (92% Pt, 8% W, available from Sigmund Cohn, of Mount Vernon, N.Y.) and titanium/nickel alloys (such as the titanium/nickel alloy known as “Nitinol”).
- bimetallic wire comprising a highly elastic metal with a highly radiopaque metal.
- a bimetallic wire would also be resistant to permanent deformation.
- An example of such a bimetallic wire is a product comprising a Nitinol outer layer and an inner core of pure reference grade platinum, available from Sigmund Cohn, of Mount Vernon, N.Y., and Anomet Products, of Shrewsbury, Mass.
- the wire 12 employed to form microcoil 14 has, for example, a diameter in the range of 0.001 to 0.005 inches.
- the microcoil 14 has a diameter that is in the range of about 0.008 to 0.016 inches.
- the axial length of the microcoil 14 may be anywhere from about 2 to 100 cm.
- the wire 12 may be larger, for example from 0.005 to 0.015 inches.
- the microcoil 14 may have a diameter in the range of about 0.010 to 0.050 inches.
- the axial length of the microcoil may be from 1 to 200 cm.
- the primary winding of the microcoil 14 is applied under tension.
- the amount of tension and the pitch of the primary winding determine the stiffness of the microcoil 14 .
- These parameters can be varied along the length of the microcoil 14 to form a microcoil having different degrees of stiffness along its length, which may be advantageous in certain applications.
- the microcoil 14 is formed into a relaxed or minimum energy state configuration by winding or otherwise manipulating the microcoil 14 about a fixture or mandrel 20 .
- the microcoil 14 and the mandrel 20 are subjected to a heat treatment, as is well known in the art. For example, an annealing temperature of about 500 degrees Celsius to about 1000 degrees Celsius is maintained for about 30 to 90 minutes, the microcoil 14 and the mandrel 20 are then cooled to room temperature and ultrasonically cleaned. The resultant secondary configuration is thereby made permanent and becomes the relaxed or minimum energy state configuration of the device 10 .
- a device or packing coil 10 employs a closed loop portion 16 and an open loop portion 18 .
- the closed loop portions 16 form substantially closed loops.
- the term “closed loop” refers to the feature in which a portion of the microcoil 14 approximately returns to or contacts another portion of the same microcoil 14 . Such a return or contact may, for example, appear as a stacking of two portions of the microcoil 14 on top of one another, as shown in FIGS. 7A, 8A, 9, and 10 .
- the substantially closed loops formed by the closed loop portion 16 may be formed in the general shape of circles, ovals or other regular geometric or irregular shapes and need not be uniformly formed within the same device 10 .
- some or all of the closed loop portions 16 may define a plane. That is to say, the closed loop portions 16 may be substantially flat and define an area or boundary through which a plane could be approximately positioned. It is further contemplated that some or all of the closed loop portions 16 may define one or more curves in the X and the Y planes. Furthermore, some or all of the closed loop portions 16 have diameters of equal lengths. In one embodiment, at least one of the diameters of the closed loop portions 16 is formed relative to a dimension of a vascular site in which the device 10 is intended to be placed. In certain embodiments of the present invention, the closed loop portions 16 have diameters of different lengths such as that shown in Fig, 10 . For example, the diameter of the closed loop portions 16 may sequentially increase, decrease, alternate between increasing and decreasing, or otherwise vary throughout the coil 10 .
- the closed loop portions 16 are, for example, formed by winding the microcoil 14 around pins 22 that project outward from the mandrel 20 one or more rotations.
- the closed loop portions 16 may be formed by winding the microcoil 14 around the pin 22 in the range of 1 to 4 rotations.
- the closed loop portions 16 may be wound about the pins 22 in either a clockwise or a counter-clockwise direction.
- the direction of the windings may but need not be uniform throughout the device 10 .
- the direction of the windings about the pins 22 of the present invention may be determined from the perspective of viewing down the length of the pin 22 with the free end of the pin 22 closest to the viewer.
- the portion of the winding furthest from the viewer i.e. on the bottom of the stack, represents the beginning of the winding and the portion closest to the viewer represents a subsequent or later portion of the winding.
- a winding or loop is formed from the bottom up relative to the mandrel 20 .
- the open loop portions 18 of the device 10 are formed in the shape of a series of open loops, curves, or waves spanning, for example as shown in FIGS. 2-4 , between two closed loop portions 16 .
- the term “open loop” refers to the feature in which a portion of the microcoil 14 folds or doubles on to itself without contacting itself, thereby leave an opening.
- the individual open loops of the open loop portion 18 may, for example, have a “C”, “U”, or “V” like form. It is noted that the individual open loops of the open looped portions 18 may be formed by winding the microcoil 14 around a portion of the pin 22 less than one full rotation.
- a single open loop portion 18 may employ three individual open loops each formed by winding the microcoil 14 about a portion of a different pin 22 and each separated from one another by an inflection point.
- a single open looped portion 18 may employ between one and 10 individual open loops.
- the form or shape of the individual open loops within a single open loop portion 18 may be the same or vary.
- the number and the form of the individual open loops employed within different open loop portions 18 may be the same or vary between different open loop portions 18 within a single device 10 .
- the height 30 of individual open loops relative to one another for example determined as the distance between sequentially formed curves of the individual open loops, may be the same or vary within a single open loop portion 18 and may be the same or vary between different open loop portions 18 within a single device 10 .
- FIG. 12 the height 30 of individual open loops relative to one another, for example determined as the distance between sequentially formed curves of the individual open loops, may be the same or vary within a single open loop portion 18 and may be the same or vary between different open loop portions 18 within a single device 10 .
- the width 32 of individual open loops relative to one another may be the same or vary within a single open loop portion 18 and may be the same or vary between different open loop portions 18 within a single device 10 .
- the open loop portions 18 may be formed substantially within a single plane, i.e. the open loop portions 18 may be substantially flat. Alternatively, the open loop portions 18 may be formed substantially within one or more curves in the X and Y planes.
- the relaxed or minimum energy state configuration of the device 10 may be formed on a mandrel 20 , for example, having a generally cube-like shape, as shown in FIGS. 3, and 5A-5C .
- FIGS. 2 and 4 show one example of a device 10 formed on such a cube-like mandrel 20 .
- FIGS. 5A-5C depict the mandrel 20 and the device 10 in simplistic line drawings. As will be noted, the pins 22 are not shown in FIGS. 5A-5C .
- FIGS. 5A-5C each show the same device 10 on the same mandrel 20 , however the mandrel is rotated 90 degrees in each subsequent figure. More particularly, FIG. 5A shows a side A facing the viewer, and FIG. 5B , in which the mandrel 20 has been rotated 90 degrees clockwise, shows the side A to the left, obscured from the viewer. Likewise, in FIG. 5C , side A is further rotated and facing away from the viewer.
- the device 10 employs four closed loop portions 16 a, 16 b, 16 c, and 16 d.
- the device is shown with two closed loop portions 16 on each side of the cube-like mandrel 20 .
- the device further employs six open loop portions 18 a, 18 b, 18 c, 18 d, 18 e, and 18 f spanning between certain pairs of the closed loop portions 16 a, 16 b, 16 c, and 16 d. It will be noted that each of the closed loop portions 16 are directly connected to three other closed loop portions 16 by three different open loop portions 18 .
- open loop portion 18 f is not shown in FIG. 3 as the open loop portion 18 f spans between closed loop portions 16 c and 16 d on the side F of the mandrel 20 that is obscured from the viewer.
- the open loop portion 18 f is shown in FIGS. 4 and 5A-5C in which the mandrel 20 is not shown or shown in a transparent manner.
- the device 10 is formed on a mandrel 20 having a shape other than a three-dimensional cube-like shape.
- the mandrel 20 may be formed in a two or three dimensional rectangular, triangular, tetrahedral, circular, oval or other regular geometric or irregular shape. It is contemplated that any number of the closed loop portions 16 and open loop portions 18 can be employed in a single device 10 of the present invention.
- the closed loop portions 16 need not form intersection-like points for a plurality of the open loop portions 18 as shown in FIGS. 2-5C . Rather the closed loop portions 16 may be formed in a sequential manner connected to one another by the open loop portions 18 , as shown in FIG. 6-8C .
- a device 90 employs only two closed loop portions 16 connected to one another by one open loop portion 18 .
- FIGS. 7A and 8A a device 110 is shown from different perspectives in a relaxed, low-energy state as the device 110 would appear on the mandrel or fixture upon which the device 110 is formed.
- FIGS. 7B and 8B show a mandrel 120 used to make the device 110 from the same perspective, respectively.
- FIGS. 7C and 8C show the device 110 on the mandrel 120 from the same perspectives, respectively.
- the pins 22 of the mandrel 120 have been omitted.
- the device 110 employs the closed loop portion 16 a that is connected to the closed loop portion 16 b by the open loop portion 18 a.
- the closed loop portion 16 b is, in turn, connected to the closed loop portion 16 c by the open loop portion 18 b. This configuration is repeated along the length of the device 110 . Stated alternatively, each closed loop portion 16 is connected to the next sequentially formed closed loop portion 16 by one open loop portion 18 .
- the device 110 is formed on the fixture or mandrel 120 .
- the mandrel 120 employs pins 22 as described above regarding the device 10 .
- the mandrel further employs one or more pins 124 that attach subassemblies 122 to one another.
- the pin 124 attaches a subassembly 122 a to a subassembly 122 b.
- the closed loop portion 16 d is formed on the pin 124 .
- the subassemblies 122 a and 122 b are formed in a generally cube-like form.
- the device 110 may employ as few as three of the closed loop portions 16 and two of the open loop portions 18 .
- the closed loop portions 16 may have diameters ranging from approximately 2 to 20 millimeters, or 3 to 15 millimeters.
- the closed loop portions 16 of the device 110 may be of a uniform diameter or may vary in diameter.
- the number and form of the open loops employed within different open loop portions 18 may be the same or vary between different open loop portions 18 within a single device 110 . For example the number of curves in a single open loop portion 18 may vary within the range of 2 to 6.
- the arc of the curves forming the individual open loops of the open loop portions 18 may also vary within a single open loop portion 18 or within a device 110 .
- the device 110 is formed by winding the microcoil 14 in the same direction for all the pins 22 on the subassembly 122 a and in an opposite direction for all the pins 22 on the subassembly 122 b.
- the devices 210 and 310 are formed on the above described mandrel 120 having the subassemblies 122 a and 122 b.
- the closed loop portion 16 d of the devices 210 and 310 are formed by winding the microcoil 14 fewer rotations than the closed loop 16 d of device 110 . More particularly, as shown in FIG. 9 , the closed loop portion 16 d of the device 210 is formed by winding the microcoil 14 , for example, approximately 1 to 1.25 rotations. As shown in FIG.
- the portion of the microcoil 14 of the device 310 that is wound around what would be pin 124 of the mandrel 20 shown in FIG. 7B is wound approximately less than one rotation.
- this portion of the microcoil 14 is referenced as portion 16 d ′ in FIG. 10 .
- the different degrees of rotations employed to form the closed loop 16 d of device 210 and the portion 16 d ′ of device 310 may be achieved by rotation of the subassembly 122 b relative to the subassembly 122 a.
- closed loop portion 16 d and the portion 16 d ′ may vary, the relative structural orientation of sequentially formed closed loop portions 16 a - 16 d, 16 a - 16 c to one another and the relative structural orientation of sequentially formed closed loop portions 16 d - 16 g, 16 e - 16 g to one another remains unchanged.
- the device 310 may be formed of a plurality of the closed loop portions 16 having, for example, diameters ranging from 3 to 15 millimeters.
- the closed loop portions 18 may, for example, be formed by winding the microcoil 14 around the pin 22 from one to 2.25 rotations.
- the device 310 may, for example, be formed of a total of three to seven closed loop portions 16 and two to six open loop portions 18 .
- the device 10 , 110 , 210 , 310 in the relaxed or minimum energy state configuration, employs a series of closed loop portions 18 and open loop portions 16 that sequentially increase or decrease in size.
- each subsequent closed loop portion 16 has a smaller diameter than the preceding closed loop portion 16 and each subsequent open loop portion 18 has a smaller height 30 and/or width 32 than the preceding open loop portion 18 .
- the devices 110 , 210 , and 310 are formed on a mandrel 120 having a shape other than that shown in FIG. 7B and 8B .
- the mandrel 120 may be formed of a single or multiple two or three dimensional rectangular, triangular, tetrahedral, circular, oval or other regular geometric or irregular shape. It is contemplated that any number of the closed loop portions 16 and open loop portions 18 can be employed in a single device 110 , 210 , and 310 of the present invention.
- the closed loop portions 16 may be formed proximate one another, i.e. the open loop portion 18 need not span between two of the closed loop portions 16 .
- the normal planes defined by sequentially formed closed loop portions 16 and open loop portions 18 are neither coincident nor parallel to one another. In certain embodiments of the present invention, the normal planes defined by sequentially formed closed loop portions 16 intersect to form a 90 degree angle or other non-zero and non-180 degree angles. In certain embodiments of the present invention, sequentially formed open loop portions and closed loop portions form an angle greater than 90 degrees and less than 180 degrees. In certain embodiments of the present invention, the normal planes defined by certain, but not necessarily all, sequentially formed open loop portions 18 intersect to form a 90 degree angle or other non-zero and non-180 degree angle.
- the open loop portions 18 of the device 10 allow for certain improvements over known occlusion devices.
- the relatively planar sections of the open loop portions 18 provide enhanced column strength to facilitate improved space seeking properties of the device 10 .
- the overall length of the open loop portions 18 allow for effective treatment of a range of target sites with a single device 10 , 110 .
- a six millimeter device 10 , 110 , 210 , 310 may be able to treat 6 to 10 millimeter aneurysms.
- the closed loop portions 16 of the device 10 , 110 , 210 , 310 provide intersecting point and ends to the open loop portions 18 that assist in preventing the formation of sudden or sharp angles within the device that may cause undesired pressure points within the target site.
- the open loop portions 18 and the closed loop portions 16 function together to provide the device or packing coil 10 , 110 , 210 , 310 , according to the present invention with improved stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for occlusion and treatment of the target site.
- a device employs a combination of any of the above disclosed features.
- the proximal end of the microcoil 14 of device is attached to the distal end of an elongate delivery device, such as a guidewire or microcatheter (not shown).
- the attachment may be by any of a number of ways known in the art, as exemplified by the following U.S. patents, the disclosures of which are expressly incorporated herein by reference: U.S. Pat. Nos. 5,108,407 to Geremia et al.; 5,122,136 to Guglielmi et al.; 5,234,437 to Sepetka; 5,261,916 to Engelson; 5,304,195 to Twyford, Jr.
- Delivery of the packing coil of the present invention may be achieved by employing features of the attachment and delivery devices described in the Assignee's of the present subject matter
- U.S. patent application Ser. No. 11/212,830 filed Aug. 25, 2005, entitled Thermal Detachment System For Implantable Devices
- a method for treating a vascular target with the device may include visualizing the target vascular site by means well-known in the art.
- the target vascular site may be, for example, an aneurysm branching off a parent artery.
- Such an aneurysm may have a dome connected to the branch artery by a neck.
- a catheter is passed intravascularly until it enters the dome of the aneurysm via the neck.
- the device is passed through the catheter with the assistance of the guidewire or microcatheter until a distal end of the device 10 enters the dome of the aneurysm.
- the device As the device enters the aneurysm, it attempts to assume its relaxed, low-energy configuration. Because the microcoil, in its relaxed configuration, is larger than the aneurysm, it is constrained into a deployed configuration in which it tends to line the periphery of the aneurysm. In this deployed configuration, the microcoil is in an energy state that is substantially higher than its relaxed, low-energy state. Thus, when the device is deployed inside a vascular site such as an aneurysm, the confinement of the device within the site causes the device to assume a three-dimensional configuration that has a higher energy state than the relaxed energy state.
- the relaxed energy state of the device is larger (in at least one dimension) than the space in which it is deployed, the deployed device is constrained by its intimate contact with the walls of the aneurysm from returning to its minimum energy state configuration. Therefore, the device engages the surrounding aneurysm wall surface, thereby minimizing shifting or tumbling due to blood flow dynamics. Furthermore, the relaxed energy state secondary configuration (to which the device attempts to revert) is not one that is conducive to “coin stacking”, thereby minimizing the degree of compaction that is experienced.
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Abstract
Description
- This application is a continuation of and claims priority to U.S. patent application Ser. No. 13/470,127 filed May 11, 2012 entitled Packing Coil, which claims benefit of and priority to U.S. Provisional Application Ser. No. 61/485,059 filed May 11, 2011 entitled Packing Coil, and to U.S. Provisional Application Ser. No. 61/536,478 filed Sep. 19, 2011 entitled Packing Coil, all of which are hereby incorporated herein by reference in their entireties.
- The present invention relates to devices for the occlusion of body cavities, such as the embolization of vascular aneurysms and the like, and methods for making and using such devices.
- The occlusion of body cavities, blood vessels, and other lumina by embolization is desired in a number of clinical situations. For example, the occlusion of fallopian tubes for the purposes of sterilization, and the occlusive repair of cardiac defects, such as a patent foramen ovale, patent ductus arteriosis, and left atrial appendage, and atrial septal defects. The function of an occlusion device in such situations is to substantially block or inhibit the flow of bodily fluids into or through the cavity, lumen, vessel, space, or defect for the therapeutic benefit of the patient.
- The embolization of blood vessels is also desired in a number of clinical situations. For example, vascular embolization has been used to control vascular bleeding, to occlude the blood supply to tumors, and to occlude vascular aneurysms, particularly intracranial aneurysms. In recent years, vascular embolization for the treatment of aneurysms has received much attention. Several different treatment modalities have been shown in the prior art. One approach that has shown promise is the use of thrombogenic microcoils. These microcoils may be made of biocompatible metal alloy(s) (typically a radio-opaque material such as platinum or tungsten) or a suitable polymer. Examples of microcoils are disclosed in the following patents: U.S. Pat. No. 4,994,069 to Ritchart et al.; U.S. Pat. No. 5,133,731 to Butler et al.; U.S. Pat. No. 5,226,911 to Chee et al.; U.S. Pat. No. 5,312,415 to Palermo; U.S. Pat. No. 5,382,259 to Phelps et al.; U.S. Pat. No. 5,382,260 to Dormandy, Jr. et al.; U.S. Pat. No. 5,476,472 to Dormandy, Jr. et al.; U.S. Pat. No. 5,578,074 to Mirigian; U.S. Pat. No. 5,582,619 to Ken; U.S. Pat. No. 5,624,461 to Mariant; U.S. Pat. No. 5,645,558 to Horton; U.S. Pat. No. 5,658,308 to Snyder; and U.S. Pat. No. 5,718,711 to Berenstein et al.; all of which are hereby incorporated by reference.
- A specific type of microcoil that has achieved a measure of success is the Guglielmi Detachable Coil (“GDC”), described in U.S. Pat. No. 5,122,136 to Guglielmi et al. The GDC employs a platinum wire coil fixed to a stainless steel delivery wire by a solder connection. After the coil is placed inside an aneurysm, an electrical current is applied to the delivery wire, which electrolytically disintegrates the solder junction, thereby detaching the coil from the delivery wire. The application of current also creates a positive electrical charge on the coil, which attracts negatively-charged blood cells, platelets, and fibrinogen, thereby increasing the thrombogenicity of the coil. Several coils of different diameters and lengths can be packed into an aneurysm until the aneurysm is completely filled. The coils thus create and hold a thrombus within the aneurysm, inhibiting its displacement and its fragmentation.
- Alternative vaso-occlusive devices are exemplified in U.S. Pat. No. 6,299,619 to Greene, Jr. et al.; U.S. Pat. No. 6,602,261 to Greene, Jr. et al.; U.S. Pat. No. 6,605,101 to Schafer et al.; U.S. Pat. No. 7,029,486 to Schaefer et al.; U.S. Pat. No. 7,033,374 to Schaefer et al.; U.S. Pat. No. 7,331,974 to Schaefer et al.; and in co-pending U.S. patent application Ser. No. 10/631,981 to Martinez; U.S. patent application Ser. No. 11/398,081 to Schaefer et al.; and U.S. patent application Ser. No. 11/398,082 to Schaefer et al., all of which are assigned to the assignee of the subject invention and incorporated herein by reference.
- There is, however, an ongoing need to provide more advanced and improved neuro-embolic microcoils that exhibit greater stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for treating and occluding the target site.
- The present invention provides a more advanced and improved occlusion device, for example an occlusion device in the form of a neuro-embolic microcoil, that exhibits greater stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for treating and occluding the target site. In one embodiment, the occlusion device comprises a microcoil having a relaxed configuration comprising a plurality of open loop portions interposed between a plurality of closed loop portions.
- In another embodiment, the occlusion device comprises a microcoil having a relaxed configuration comprising a plurality of open loop portions interposed between a plurality of closed loop portions, each of the plurality of open looped portions formed substantially within a different plane.
- In another embodiment, the present invention provides a method for occluding a body cavity comprising passing a delivery system through a vasculature until a distal end of the delivery system is positioned at a target location; advancing a first portion of the occlusion device from the distal end of the delivery system into the target site, the first portion forming a closed loop when the occlusion device is in a relaxed state; advancing a second portion of the occlusion device from the distal end of the delivery system into the target site, the second portion forming at least one open loop when the occlusion device is in a relaxed state; advancing a third portion of the occlusion device from the distal end of the delivery system into the target site, the first portion forming a closed loop when the occlusion device is in a relaxed state; and releasing the occlusion device from the delivery system and withdrawing the delivery system from the vasculature.
- These and other aspects, features and advantages of which embodiments of the invention are capable of will be apparent and elucidated from the following description of embodiments of the present invention, reference being made to the accompanying drawings, in which
-
FIG. 1 is a perspective view of a portion of a microcoil employed to form a device according to the present invention; -
FIG. 2 is a perspective view of device according to one embodiment of the present invention. -
FIG. 3 is a perspective view of a device on a mandrel employed to fabricate the device according to one embodiment of the present invention; -
FIG. 4 is a perspective view of a device according to one embodiment of the present invention. -
FIGS. 5A through 5C are perspective views of a device on a mandrel employed to fabricate the device according to one embodiment of the present invention. -
FIG. 6 is a perspective view of a device according to one embodiment of the present invention. -
FIG. 7A is a perspective view of a device according to one embodiment of the present invention. -
FIG. 7B is a perspective view of a mandrel employed to fabricate a device according to one embodiment of the present invention. -
FIG. 7C is a perspective view of a device on a mandrel according to one embodiment of the present invention. -
FIG. 8A is a perspective view of a device according to one embodiment of the present invention. -
FIG. 8B is a perspective view of a mandrel employed to fabricate a device according to one embodiment of the present invention. -
FIG. 8C is a perspective view of a device on a mandrel according to one embodiment of the present invention. -
FIG. 9 is a perspective view of a device according to one embodiment of the present invention. -
FIG. 10 is a perspective view of a device according to one embodiment of the present invention. -
FIG. 11 is a table describing various configurations of a device according to one embodiment of the present invention. -
FIG. 12 is a perspective view of a device according to one embodiment of the present invention. - Specific embodiments of the invention will now be described with reference to the accompanying drawings. This invention may, however, be embodied in many different forms and should not be construed as limited to the embodiments set forth herein; rather, these embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the invention to those skilled in the art. The terminology used in the detailed description of the embodiments illustrated in the accompanying drawings is not intended to be limiting of the invention. In the drawings, like numbers refer to like elements.
- Devices or packing coils according to the present invention provide improved stability after deployment in a target site; improved space seeking ability within the target site; wider application for treatment of target sites of varying sizes; and increased efficacy for occlusion and treatment of the target site. Broadly speaking, these objectives are achieved by employing a microcoil having a relaxed, low-energy state configuration incorporating both closed loop portions and open loop portions.
- With reference to
FIG. 1 , devices or packing coils according to the present invention are formed of a suitable length ofwire 12 formed into a primary winding in the shape of ahelical microcoil 14. Suitable materials for thewire 12 include platinum, rhodium, palladium, rhenium, tungsten, gold, silver, tantalum, and various alloys of these metals. Various surgical grade stainless steels may also be used. Preferred materials include the platinum/tungsten alloy known as Platinum 479 (92% Pt, 8% W, available from Sigmund Cohn, of Mount Vernon, N.Y.) and titanium/nickel alloys (such as the titanium/nickel alloy known as “Nitinol”). Another material that may be advantageous is a bimetallic wire comprising a highly elastic metal with a highly radiopaque metal. Such a bimetallic wire would also be resistant to permanent deformation. An example of such a bimetallic wire is a product comprising a Nitinol outer layer and an inner core of pure reference grade platinum, available from Sigmund Cohn, of Mount Vernon, N.Y., and Anomet Products, of Shrewsbury, Mass. - In embodiments useful for treating neurovascular malformations, the
wire 12 employed to formmicrocoil 14 has, for example, a diameter in the range of 0.001 to 0.005 inches. Themicrocoil 14 has a diameter that is in the range of about 0.008 to 0.016 inches. The axial length of themicrocoil 14 may be anywhere from about 2 to 100 cm. In embodiments useful for treating larger maliformations that may occur in the peripheral vasculature, thewire 12 may be larger, for example from 0.005 to 0.015 inches. Themicrocoil 14 may have a diameter in the range of about 0.010 to 0.050 inches. The axial length of the microcoil may be from 1 to 200 cm. Those skilled in the art will appreciate that the wire size, coil diameter, and length are a matter of design selection and are usually scaled to the malformation intended to be treated. - The primary winding of the
microcoil 14 is applied under tension. The amount of tension and the pitch of the primary winding determine the stiffness of themicrocoil 14. These parameters can be varied along the length of the microcoil 14 to form a microcoil having different degrees of stiffness along its length, which may be advantageous in certain applications. - The
microcoil 14 is formed into a relaxed or minimum energy state configuration by winding or otherwise manipulating themicrocoil 14 about a fixture ormandrel 20. Once associated with themandrel 20, themicrocoil 14 and themandrel 20 are subjected to a heat treatment, as is well known in the art. For example, an annealing temperature of about 500 degrees Celsius to about 1000 degrees Celsius is maintained for about 30 to 90 minutes, themicrocoil 14 and themandrel 20 are then cooled to room temperature and ultrasonically cleaned. The resultant secondary configuration is thereby made permanent and becomes the relaxed or minimum energy state configuration of thedevice 10. - With reference to
FIG. 2 , a device or packingcoil 10 according to one embodiment of the present invention employs aclosed loop portion 16 and anopen loop portion 18. Theclosed loop portions 16 form substantially closed loops. The term “closed loop” refers to the feature in which a portion of the microcoil 14 approximately returns to or contacts another portion of thesame microcoil 14. Such a return or contact may, for example, appear as a stacking of two portions of themicrocoil 14 on top of one another, as shown inFIGS. 7A, 8A, 9, and 10 . The substantially closed loops formed by theclosed loop portion 16 may be formed in the general shape of circles, ovals or other regular geometric or irregular shapes and need not be uniformly formed within thesame device 10. - As shown in
FIGS. 2-4 , some or all of theclosed loop portions 16 may define a plane. That is to say, theclosed loop portions 16 may be substantially flat and define an area or boundary through which a plane could be approximately positioned. It is further contemplated that some or all of theclosed loop portions 16 may define one or more curves in the X and the Y planes. Furthermore, some or all of theclosed loop portions 16 have diameters of equal lengths. In one embodiment, at least one of the diameters of theclosed loop portions 16 is formed relative to a dimension of a vascular site in which thedevice 10 is intended to be placed. In certain embodiments of the present invention, theclosed loop portions 16 have diameters of different lengths such as that shown in Fig, 10. For example, the diameter of theclosed loop portions 16 may sequentially increase, decrease, alternate between increasing and decreasing, or otherwise vary throughout thecoil 10. - The
closed loop portions 16 are, for example, formed by winding themicrocoil 14 aroundpins 22 that project outward from themandrel 20 one or more rotations. For example, theclosed loop portions 16 may be formed by winding themicrocoil 14 around thepin 22 in the range of 1 to 4 rotations. Theclosed loop portions 16 may be wound about thepins 22 in either a clockwise or a counter-clockwise direction. The direction of the windings may but need not be uniform throughout thedevice 10. The direction of the windings about thepins 22 of the present invention may be determined from the perspective of viewing down the length of thepin 22 with the free end of thepin 22 closest to the viewer. Where themicrocoil 14 is stacked upon itself, the portion of the winding furthest from the viewer, i.e. on the bottom of the stack, represents the beginning of the winding and the portion closest to the viewer represents a subsequent or later portion of the winding. Stated alternatively, a winding or loop is formed from the bottom up relative to themandrel 20. - The
open loop portions 18 of thedevice 10 are formed in the shape of a series of open loops, curves, or waves spanning, for example as shown inFIGS. 2-4 , between twoclosed loop portions 16. The term “open loop” refers to the feature in which a portion of the microcoil 14 folds or doubles on to itself without contacting itself, thereby leave an opening. The individual open loops of theopen loop portion 18 may, for example, have a “C”, “U”, or “V” like form. It is noted that the individual open loops of the open loopedportions 18 may be formed by winding themicrocoil 14 around a portion of thepin 22 less than one full rotation. For example, a singleopen loop portion 18 may employ three individual open loops each formed by winding themicrocoil 14 about a portion of adifferent pin 22 and each separated from one another by an inflection point. A single open loopedportion 18 may employ between one and 10 individual open loops. - The form or shape of the individual open loops within a single
open loop portion 18 may be the same or vary. The number and the form of the individual open loops employed within differentopen loop portions 18 may be the same or vary between differentopen loop portions 18 within asingle device 10. As shown inFIG. 12 , theheight 30 of individual open loops relative to one another, for example determined as the distance between sequentially formed curves of the individual open loops, may be the same or vary within a singleopen loop portion 18 and may be the same or vary between differentopen loop portions 18 within asingle device 10. As also shown inFIG. 12 , thewidth 32 of individual open loops relative to one another, for example determined as the distance between the inflection points of sequentially formed individual open loops, may be the same or vary within a singleopen loop portion 18 and may be the same or vary between differentopen loop portions 18 within asingle device 10. - As shown in
FIGS. 2- 7A, 7C, 8A, 8C, 9, and 10, the5C open loop portions 18 may be formed substantially within a single plane, i.e. theopen loop portions 18 may be substantially flat. Alternatively, theopen loop portions 18 may be formed substantially within one or more curves in the X and Y planes. - In one embodiment of the present invention, the relaxed or minimum energy state configuration of the
device 10 may be formed on amandrel 20, for example, having a generally cube-like shape, as shown inFIGS. 3, and 5A-5C .FIGS. 2 and 4 show one example of adevice 10 formed on such a cube-like mandrel 20. - For the sake of clarity, the
pins 22 indicated inFIG. 3 are shown as voids rather than pins projecting out from themandrel 20. Also for the sake of clarity,FIGS. 5A-5C depict themandrel 20 and thedevice 10 in simplistic line drawings. As will be noted, thepins 22 are not shown inFIGS. 5A-5C . In order to better show thedevice 10,FIGS. 5A-5C each show thesame device 10 on thesame mandrel 20, however the mandrel is rotated 90 degrees in each subsequent figure. More particularly,FIG. 5A shows a side A facing the viewer, andFIG. 5B , in which themandrel 20 has been rotated 90 degrees clockwise, shows the side A to the left, obscured from the viewer. Likewise, inFIG. 5C , side A is further rotated and facing away from the viewer. - As shown in
FIGS. 5A-5C , thedevice 10 employs fourclosed loop portions closed loop portions 16 on each side of the cube-like mandrel 20. The device further employs sixopen loop portions closed loop portions closed loop portions 16 are directly connected to three otherclosed loop portions 16 by three differentopen loop portions 18. - It is further noted that the
open loop portion 18 f is not shown inFIG. 3 as theopen loop portion 18 f spans betweenclosed loop portions mandrel 20 that is obscured from the viewer. Theopen loop portion 18 f is shown inFIGS. 4 and 5A-5C in which themandrel 20 is not shown or shown in a transparent manner. - In certain embodiments of the present invention, the
device 10 is formed on amandrel 20 having a shape other than a three-dimensional cube-like shape. For example, themandrel 20 may be formed in a two or three dimensional rectangular, triangular, tetrahedral, circular, oval or other regular geometric or irregular shape. It is contemplated that any number of theclosed loop portions 16 andopen loop portions 18 can be employed in asingle device 10 of the present invention. - In certain other embodiments of the present invention, the
closed loop portions 16 need not form intersection-like points for a plurality of theopen loop portions 18 as shown inFIGS. 2-5C . Rather theclosed loop portions 16 may be formed in a sequential manner connected to one another by theopen loop portions 18, as shown inFIG. 6-8C . For example, as shown inFIG. 6 , adevice 90 employs only two closedloop portions 16 connected to one another by oneopen loop portion 18. - In another example, as shown in
FIGS. 7A and 8A , adevice 110 is shown from different perspectives in a relaxed, low-energy state as thedevice 110 would appear on the mandrel or fixture upon which thedevice 110 is formed.FIGS. 7B and 8B show amandrel 120 used to make thedevice 110 from the same perspective, respectively.FIGS. 7C and 8C show thedevice 110 on themandrel 120 from the same perspectives, respectively. However, for the sake of clarity, thepins 22 of themandrel 120 have been omitted. Thedevice 110 employs the closedloop portion 16 a that is connected to theclosed loop portion 16 b by theopen loop portion 18 a. Theclosed loop portion 16 b is, in turn, connected to theclosed loop portion 16 c by the open loop portion 18 b. This configuration is repeated along the length of thedevice 110. Stated alternatively, eachclosed loop portion 16 is connected to the next sequentially formedclosed loop portion 16 by oneopen loop portion 18. - As shown in
FIG. 7B and 8B , thedevice 110 is formed on the fixture ormandrel 120. Themandrel 120 employspins 22 as described above regarding thedevice 10. The mandrel further employs one ormore pins 124 that attach subassemblies 122 to one another. Thepin 124 attaches asubassembly 122 a to a subassembly 122 b. In order to more easily relateFIGS. 7A-8C to one another, it is noted that theclosed loop portion 16 d is formed on thepin 124. Thesubassemblies 122 a and 122 b are formed in a generally cube-like form. However, for the sake of clarity, it is noted that the corners of thesubassemblies 122 a and 122 b that do not employ thepin subassemblies 122 a and 122 b. - It is noted that while the
device 110 is shown as employing seven of theclosed loop portions 16 and six of theopen loop portions 18, thedevice 110 may employ as few as three of theclosed loop portions 16 and two of theopen loop portions 18. Theclosed loop portions 16 may have diameters ranging from approximately 2 to 20 millimeters, or 3 to 15 millimeters. Theclosed loop portions 16 of thedevice 110 may be of a uniform diameter or may vary in diameter. The number and form of the open loops employed within differentopen loop portions 18 may be the same or vary between differentopen loop portions 18 within asingle device 110. For example the number of curves in a singleopen loop portion 18 may vary within the range of 2 to 6. The arc of the curves forming the individual open loops of theopen loop portions 18 may also vary within a singleopen loop portion 18 or within adevice 110. - In one embodiment of the present invention, the
device 110 is formed by winding themicrocoil 14 in the same direction for all thepins 22 on thesubassembly 122 a and in an opposite direction for all thepins 22 on the subassembly 122 b. - In another embodiment of the present invention, the
devices FIGS. 9 and 10 respectively, are formed on the above describedmandrel 120 having thesubassemblies 122 a and 122 b. However, as best seen through a comparison ofFIG. 7A andFIGS. 9 and 10 , theclosed loop portion 16 d of thedevices microcoil 14 fewer rotations than the closedloop 16 d ofdevice 110. More particularly, as shown inFIG. 9 , theclosed loop portion 16 d of thedevice 210 is formed by winding themicrocoil 14, for example, approximately 1 to 1.25 rotations. As shown inFIG. 10 , the portion of themicrocoil 14 of thedevice 310 that is wound around what would be pin 124 of themandrel 20 shown inFIG. 7B , is wound approximately less than one rotation. For the sake of clarity, this portion of themicrocoil 14 is referenced asportion 16 d′ inFIG. 10 . It is noted that the different degrees of rotations employed to form theclosed loop 16 d ofdevice 210 and theportion 16 d′ ofdevice 310 may be achieved by rotation of the subassembly 122 b relative to thesubassembly 122 a. Accordingly, it is noted that while the number of rotations employed to form closedloop portion 16 d and theportion 16 d′ may vary, the relative structural orientation of sequentially formedclosed loop portions 16 a-16 d, 16 a-16 c to one another and the relative structural orientation of sequentially formedclosed loop portions 16 d-16 g, 16 e-16 g to one another remains unchanged. - Described in Table 1 shown in
FIG. 11 are various exemplary configurations of thedevice 310 according to the present invention. As can be seen, thedevice 310 may be formed of a plurality of theclosed loop portions 16 having, for example, diameters ranging from 3 to 15 millimeters. Theclosed loop portions 18 may, for example, be formed by winding themicrocoil 14 around thepin 22 from one to 2.25 rotations. Thedevice 310 may, for example, be formed of a total of three to sevenclosed loop portions 16 and two to sixopen loop portions 18. - In another embodiment of the present invention, as shown in
FIG. 12 , thedevice loop portions 18 andopen loop portions 16 that sequentially increase or decrease in size. For example, each subsequentclosed loop portion 16 has a smaller diameter than the precedingclosed loop portion 16 and each subsequentopen loop portion 18 has asmaller height 30 and/orwidth 32 than the precedingopen loop portion 18. - In certain embodiments of the present invention, the
devices mandrel 120 having a shape other than that shown inFIG. 7B and 8B . For example, themandrel 120 may be formed of a single or multiple two or three dimensional rectangular, triangular, tetrahedral, circular, oval or other regular geometric or irregular shape. It is contemplated that any number of theclosed loop portions 16 andopen loop portions 18 can be employed in asingle device - In certain other embodiments of the present invention, the
closed loop portions 16 may be formed proximate one another, i.e. theopen loop portion 18 need not span between two of theclosed loop portions 16. - In certain embodiments of the present invention, the normal planes defined by sequentially formed
closed loop portions 16 andopen loop portions 18 are neither coincident nor parallel to one another. In certain embodiments of the present invention, the normal planes defined by sequentially formedclosed loop portions 16 intersect to form a 90 degree angle or other non-zero and non-180 degree angles. In certain embodiments of the present invention, sequentially formed open loop portions and closed loop portions form an angle greater than 90 degrees and less than 180 degrees. In certain embodiments of the present invention, the normal planes defined by certain, but not necessarily all, sequentially formedopen loop portions 18 intersect to form a 90 degree angle or other non-zero and non-180 degree angle. - It is believed that the
open loop portions 18 of thedevice 10 allow for certain improvements over known occlusion devices. For example, the relatively planar sections of theopen loop portions 18 provide enhanced column strength to facilitate improved space seeking properties of thedevice 10. Additionally, the overall length of theopen loop portions 18 allow for effective treatment of a range of target sites with asingle device millimeter device - With respect to the
closed loop portions 16 of thedevice closed loop portions 16 provide intersecting point and ends to theopen loop portions 18 that assist in preventing the formation of sudden or sharp angles within the device that may cause undesired pressure points within the target site. - Accordingly, the
open loop portions 18 and theclosed loop portions 16 function together to provide the device or packingcoil - In alternative embodiments of devices according to the present invention, a device employs a combination of any of the above disclosed features.
- In order to deliver the device of the present invention to a target, such as an aneurysm, the proximal end of the
microcoil 14 of device is attached to the distal end of an elongate delivery device, such as a guidewire or microcatheter (not shown). The attachment may be by any of a number of ways known in the art, as exemplified by the following U.S. patents, the disclosures of which are expressly incorporated herein by reference: U.S. Pat. Nos. 5,108,407 to Geremia et al.; 5,122,136 to Guglielmi et al.; 5,234,437 to Sepetka; 5,261,916 to Engelson; 5,304,195 to Twyford, Jr. et al.; 5,312,415 to Palermo; 5,423,829 to Pham et al.; 5,522,836 to Palermo; 5,645,564 to Northrup et al.; 5,725,546 to Samson; 5,800,453 to Gia; 5,814,062 to Sepetka et al.; 5,911,737 to Lee et al.; 5,989,242 to Saadat et al.; 6,022,369 to Jacobsen et al.; 6,063,100 to Diaz et al.; 6,068,644 to Lulo et al.; and 6,102,933 to Lee et al. - Delivery of the packing coil of the present invention may be achieved by employing features of the attachment and delivery devices described in the Assignee's of the present subject matter U.S. Provisional Application Ser. No. 60/604,671, filed Aug. 25, 2004, entitled Thermal Detachment System For Implantable Devices; U.S. Provisional Application Ser. No. 60/685,342 filed May 27, 2005, entitled Thermal Detachment System For Implantable Devices; U.S. patent application Ser. No. 11/212,830 filed Aug. 25, 2005, entitled Thermal Detachment System For Implantable Devices; U.S. Provisional Application Ser. No. 60/952,520 filed Jul. 27, 2007, entitled Detachable Coil Incorporating Stretch Resistance; U.S. Provisional Application Ser. No. 61/016,154 filed Dec. 21, 2007, entitled System and Method For Locating Detachment Zone Of A Detachable Implant; and U.S. Provisional Application Ser. No. 61/324,246 filed Apr. 14, 2010, entitled Implant Delivery Device which are each herein incorporated in their entirety by reference.
- A method for treating a vascular target with the device may include visualizing the target vascular site by means well-known in the art. The target vascular site may be, for example, an aneurysm branching off a parent artery. Such an aneurysm may have a dome connected to the branch artery by a neck. A catheter is passed intravascularly until it enters the dome of the aneurysm via the neck. The device is passed through the catheter with the assistance of the guidewire or microcatheter until a distal end of the
device 10 enters the dome of the aneurysm. - As the device enters the aneurysm, it attempts to assume its relaxed, low-energy configuration. Because the microcoil, in its relaxed configuration, is larger than the aneurysm, it is constrained into a deployed configuration in which it tends to line the periphery of the aneurysm. In this deployed configuration, the microcoil is in an energy state that is substantially higher than its relaxed, low-energy state. Thus, when the device is deployed inside a vascular site such as an aneurysm, the confinement of the device within the site causes the device to assume a three-dimensional configuration that has a higher energy state than the relaxed energy state. Because the relaxed energy state of the device is larger (in at least one dimension) than the space in which it is deployed, the deployed device is constrained by its intimate contact with the walls of the aneurysm from returning to its minimum energy state configuration. Therefore, the device engages the surrounding aneurysm wall surface, thereby minimizing shifting or tumbling due to blood flow dynamics. Furthermore, the relaxed energy state secondary configuration (to which the device attempts to revert) is not one that is conducive to “coin stacking”, thereby minimizing the degree of compaction that is experienced.
- Although the invention has been described in terms of particular embodiments and applications, one of ordinary skill in the art, in light of this teaching, can generate additional embodiments and modifications without departing from the spirit of or exceeding the scope of the claimed invention. Accordingly, it is to be understood that the drawings and descriptions herein are proffered by way of example to facilitate comprehension of the invention and should not be construed to limit the scope thereof.
Claims (14)
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US10028747B2 (en) | 2008-05-01 | 2018-07-24 | Aneuclose Llc | Coils with a series of proximally-and-distally-connected loops for occluding a cerebral aneurysm |
US10716573B2 (en) | 2008-05-01 | 2020-07-21 | Aneuclose | Janjua aneurysm net with a resilient neck-bridging portion for occluding a cerebral aneurysm |
CN102361602B (en) | 2009-01-22 | 2017-04-26 | 康奈尔大学 | Method and apparatus for restricting flow through the wall of lumen |
US9358140B1 (en) | 2009-11-18 | 2016-06-07 | Aneuclose Llc | Stent with outer member to embolize an aneurysm |
US9211396B2 (en) | 2010-02-23 | 2015-12-15 | Covidien Lp | Devices and methods for vascular recanalization |
EP2693981A4 (en) * | 2011-04-01 | 2015-07-01 | Univ Cornell | Method and apparatus for restricting flow through an opening in the side wall of a body lumen, and/or for reinforcing a weakness in the side wall of a body lumen, while still maintaining substantially normal flow through the body lumen |
AU2012253287B2 (en) * | 2011-05-11 | 2016-11-24 | Microvention, Inc. | Packing coil |
US20150327868A1 (en) | 2014-05-13 | 2015-11-19 | Ndi Tip Teknolojileri Anonim Sirketi | Retractable and rapid disconnect, floating diameter embolic coil product and delivery system |
JP6782251B2 (en) * | 2015-11-19 | 2020-11-11 | 株式会社カネカ | In-vivo indwelling member and in-vivo indwelling member arranging device including the in-vivo indwelling member |
CN108814669B (en) * | 2018-10-09 | 2019-02-05 | 微创神通医疗科技(上海)有限公司 | Embolization device and its spring ring |
US11399840B2 (en) | 2019-08-13 | 2022-08-02 | Covidien Lp | Implantable embolization device |
WO2022040683A1 (en) * | 2020-08-18 | 2022-02-24 | Balt Usa, Llc | Vascular embolic implant |
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US10299798B2 (en) * | 2011-05-11 | 2019-05-28 | Microvention, Inc. | Packing coil |
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US20100234872A1 (en) * | 2009-03-13 | 2010-09-16 | Boston Scientific Scimed, Inc. | Electrical contact for occlusive device delivery system |
US10299798B2 (en) * | 2011-05-11 | 2019-05-28 | Microvention, Inc. | Packing coil |
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EP2707078B1 (en) | 2017-07-05 |
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CA2835430C (en) | 2018-07-31 |
KR101837798B1 (en) | 2018-03-12 |
KR20140033374A (en) | 2014-03-18 |
JP6157453B2 (en) | 2017-07-05 |
CN103826688A (en) | 2014-05-28 |
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